Talaromyces flavus and application of same in prevention of plant pathogens
A yellow taromycetes, plant pathogenic bacteria technology, applied in the application, plant growth regulators, botanical equipment and methods, etc., can solve problems such as serious disease occurrence, environmental pollution, etc., to improve quality and yield, prevent environmental pollution, Significant economic and social benefits
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Embodiment 1
[0028] Embodiment 1: Isolation of antagonistic bacteria
[0029] The study found that the peanut rhizosphere soil after 4 years of continuous cropping in Laixi City, Shandong Province, compared with the peanut rhizosphere soil of 2 and 7 years of continuous cropping, the species and number of plant pathogens were significantly reduced, the obstacles to continuous cropping of peanuts were significantly reduced, and the yield and quality were improved. The rhizosphere soil of peanuts in continuous cropping for 4 years in Laixi City, Shandong Province was separated by dilution separation method. The yellow-blue bacteria described in the present invention are isolated from the rhizosphere soil of peanuts in continuous cropping for 4 years. By purifying the single spores of the isolates, they are inoculated with common plant pathogenic bacteria at two points on the PDA plate respectively, and the plate antagonism test is carried out. Filtered to get.
Embodiment 2
[0030] Embodiment 2, identification of antagonistic bacteria
[0031] 1. Morphological identification of antagonistic bacteria
[0032] The medium used in the experiment is as follows:
[0033] (1) Chase agar (CA): 3.0g sodium nitrate, 1.0g dipotassium hydrogen phosphate, 0.5g potassium chloride, 0.5g magnesium sulfate heptahydrate, 0.01g ferrous sulfate heptahydrate, 30g sucrose, 15g agar, distilled water 1000mL, heated to dissolve, and finally adjusted to 1000mL, sterilized at 121°C for 15min.
[0034] (2) Chabai Yeast Extract Agar (CYA): 10mL of Chabai concentrated stock solution, 1.0g of dipotassium hydrogen phosphate, 5g of yeast extract, 30g of sucrose, 15g of agar, 1000mL of distilled water, heat to dissolve, and finally dilute to 1000mL. Sterilize at 121°C for 15 minutes.
[0035] Cha's concentrated stock solution: 30g of sodium nitrate, 5g of potassium chloride, 5g of magnesium sulfate heptahydrate, 0.1g of ferrous sulfate heptahydrate, 100mL of water, heated to di...
Embodiment 3
[0055] Embodiment 3, the bacteriostasis of yellow basket bacterium.
[0056] The yellow basket fungus was inoculated with plant pathogenic fungi such as Chestnut Phytophthora, Curvularia maize leaf spot, Wheat Scab, Tobacco Alternaria Alternaria, Poplar Rot and Rhizoctonia solani and other plant pathogenic fungi using a two-point confrontation method. At the same time, the PDA plate inoculated with each pathogenic bacteria was used as a control. Place in a constant temperature and humidity incubator at 28°C for culture, and measure the colony diameter 3 days after inoculation until the control plate is covered with the plate. The antibacterial rate was calculated, and the results are shown in Table 1.
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